The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes-Reference-Cited by-同舟云学术

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The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes

Published:1992-08-21 Issue:5073 Volume:257 Page:1121-1124
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Gardner John M.¹,Nakatsu Yoshimichi¹,Gondo Yoichi¹,Lee Susan¹,Lyon Mary F.²,King Richard A.³,Brilliant Murray H.¹

Affiliation:

1. The Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111

2. Radiobiology Unit, Medical Research Council, Chilton, Didcot, Oxon OX11 ORD, United Kingdom

3. Department of Medicine, University of Minnesota, Minneapolis, MN 55455

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference50 articles.

1. APKARIAN, P, VISUAL EVOKED-POTENTIALS IN PRADER-WILLI SYNDROME, DOCUMENTA OPHTHALMOLOGICA 71: 355 (1989).

2. BRAY, G.A., THE PRADER-WILLI SYNDROME - A STUDY OF 40 PATIENTS AND A REVIEW OF THE LITERATURE, MEDICINE 62: 59 (1983).

3. BRILLIANT, M.H., THE MOUSE PINK-EYED DILUTION LOCUS - A MODEL FOR ASPECTS OF PRADER-WILLI SYNDROME, ANGELMAN SYNDROME, AND A FORM OF HYPOMELANOSIS OF ITO, MAMMALIAN GENOME 3: 187 (1992).

4. Direct Molecular Identification of the Mouse Pink-Eyed Unstable Mutation by Genome Scanning

5. BRILLIANT M.H. unpublished data.

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